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Rxivist combines preprints from bioRxiv with data from Twitter to help you find the papers being discussed in your field. Currently indexing 62,747 bioRxiv papers from 278,434 authors.

Author: Naomi R. Wray

Rankings

  • All-time downloads: 77,193 (rank: 155 out of 278,434)
  • Categories:
    • bioinformatics: 4,762 (rank: 1,192 out of 24,395)
    • epidemiology: 201 (rank: 5,778 (tie) out of 9,529)
    • genetics: 59,208 (rank: 46 out of 27,725)
    • genomics: 12,318 (rank: 722 out of 31,945)
    • neuroscience: 704 (rank: 13,803 (tie) out of 45,895)

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Preprints

Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression

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New mutations, old statistical challenges

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Genomewide association study identifies 30 loci associated with bipolar disorder

genetics more details view paper
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Regulatory variants explain much more heritability than coding variants across 11 common diseases

genetics more details view paper
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Genome-wide meta-analysis of depression identifies 102 independent variants and highlights the importance of the prefrontal brain regions.

genetics more details view paper
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Contrasting regional architectures of schizophrenia and other complex diseases using fast variance components analysis

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Haplotypes of common SNPs can explain missing heritability of complex diseases

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Genome wide meta-analysis identifies genomic relationships, novel loci, and pleiotropic mechanisms across eight psychiatric disorders.

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Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank

genomics more details view paper
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Commentary on "Limitations of GCTA as a solution to the missing heritability problem"

genetics more details view paper
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Common schizophrenia alleles are enriched in mutation-intolerant genes and maintained by background selection

genomics more details view paper
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A comparative study of techniques for differential expression analysis on RNA-Seq data

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Improved polygenic prediction by Bayesian multiple regression on summary statistics

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Widespread signatures of negative selection in the genetic architecture of human complex traits

genetics more details view paper
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GWAS on family history of Alzheimer's disease

genetics more details view paper
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A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects

genetics more details view paper
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Causal associations between risk factors and common diseases inferred from GWAS summary data

genetics more details view paper
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A resource-efficient tool for mixed model association analysis of large-scale data

genetics more details view paper
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    • In genetics: 370 out of 3,562
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Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

genomics more details view paper
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    • Site-wide: 37,660 out of 62,747

Imprint of Assortative Mating on the Human Genome

genetics more details view paper
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Genotype-by-environment interactions inferred from genetic effects on phenotypic variability in the UK Biobank

genetics more details view paper
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Improved prediction of chronological age from DNA methylation limits it as a biomarker of ageing

bioinformatics more details view paper
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    • In bioinformatics: 1,333 out of 6,251
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OSCA: a tool for omic-data-based complex trait analysis

bioinformatics more details view paper
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    • In bioinformatics: 1,372 out of 6,251
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Estimation of genetic correlation using linkage disequilibrium score regression and genomic restricted maximum likelihood

genetics more details view paper
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    • In genetics: 626 out of 3,562
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Identification of 55,000 Replicated DNA Methylation QTL

genomics more details view paper
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Epigenetic prediction of complex traits and death

genomics more details view paper
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The Project MinE databrowser: bringing large-scale whole-genome sequencing in ALS to researchers and the public

genomics more details view paper
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GWAS of epigenetic ageing rates in blood reveals a critical role for TERT

genetics more details view paper
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    • In genetics: 865 out of 3,562
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Identifying gene targets for brain-related traits using transcriptomic and methylomic data from blood

genetics more details view paper
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Genome-wide association study of suicide attempt in psychiatric disorders identifies association with major depression polygenic risk scores

genetics more details view paper
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Genetic stratification of depression in UK Biobank suggests a subgroup linked to age of natural menopause

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Bayesian reassessment of the epigenetic architecture of complex traits

genomics more details view paper
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Evidence of causal effect of major depression on alcohol dependence: Findings from the Psychiatric Genomics Consortium

genetics more details view paper
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DEAR-O: Differential Expression Analysis based on RNA-seq data - Online

bioinformatics more details view paper
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Comparison of Genotypic and Phenotypic Correlations: Cheverud’s Conjecture in Humans

genetics more details view paper
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Across-cohort QC analyses of genome-wide association study summary statistics from complex traits

genetics more details view paper
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Genotype-covariate correlation and interaction disentangled by a whole-genome multivariate reaction norm model

genetics more details view paper
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Conditional GWAS analysis identifies putative disorder-specific SNPs for psychiatric disorders

genetics more details view paper
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Widespread associations between grey matter structure and the human phenome

neuroscience more details view paper
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Bayesian analysis of GWAS summary data reveals differential signatures of natural selection across human complex traits and functional genomic categories

genetics more details view paper
  • Downloaded 420 times
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    • Site-wide: 254 out of 62,747

Age at first birth in women is genetically associated with increased risk of schizophrenia

genetics more details view paper
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A better design for stratified medicine based on genomic prediction

genetics more details view paper
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The Australian Genetics of Depression Study: Study Description and Sample Characteristics

genetics more details view paper
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Genetic analyses of medication-use and implications for precision medicine

genetics more details view paper
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    • Site-wide: 35,226 out of 62,747

Promoter-anchored chromatin interactions predicted from genetic analysis of epigenomic data

genetics more details view paper
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    • Site-wide: 43,569 out of 62,747

Exploring contributors to variability in estimates of SNP-heritability and genetic correlations from the iPSYCH case-cohort and published meta-studies of major psychiatric disorders.

genetics more details view paper
  • Downloaded 284 times
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Genetic and epigenetic architectures of neurological protein biomarkers in the Lothian Birth Cohort 1936

neuroscience more details view paper
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    • Site-wide: 27,322 out of 62,747

Cross-disorder GWAS meta-analysis for Attention Deficit/Hyperactivity Disorder, Autism Spectrum Disorder, Obsessive Compulsive Disorder, and Tourette Syndrome

genetics more details view paper
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    • Site-wide: 981 out of 62,747

Trajectories of inflammatory biomarkers over the eighth decade and their associations with immune cell counts and epigenetic ageing

epidemiology more details view paper
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